Blouin J - Search Results

1

[Neisseria meningitidis infection. Clinical criteria orienting towards a deficiency in the proteins of the complement].

Rameix-Welti MA, Chedani H, Blouin J, Alonso JM, Fridman WH, Fremeaux-Bacchi V. Rameix-Welti MA, et al. Among authors: blouin j. Presse Med. 2005 Mar 26;34(6):425-30. doi: 10.1016/s0755-4982(05)83936-3. Presse Med. 2005. PMID: 15902872 French.

2

[Investigation of the complement system in clinical practice].

Frémeaux-Bacchi V, Dragon-Durey MA, Blouin J, Mouthon L, Fridman WH. Frémeaux-Bacchi V, et al. Among authors: blouin j. Ann Med Interne (Paris). 2003 Dec;154(8):529-40. Ann Med Interne (Paris). 2003. PMID: 15037829 Review. French.

3

Hereditary complement C7 deficiency in nine families: subtotal C7 deficiency revisited.

Rameix-Welti MA, Régnier CH, Bienaimé F, Blouin J, Schifferli J, Fridman WH, Sautès-Fridman C, Frémeaux-Bacchi V. Rameix-Welti MA, et al. Among authors: blouin j. Eur J Immunol. 2007 May;37(5):1377-85. doi: 10.1002/eji.200636812. Eur J Immunol. 2007. PMID: 17407100 Free article.

4

[Partial properdin deficiency revealed by a septicemia caused by Neisseria meningitidis].

Frémeaux-Bacchi V, Le Coustumier A, Blouin J, Kazatchkine MD, Weiss L. Frémeaux-Bacchi V, et al. Among authors: blouin j. Presse Med. 1995 Sep 30;24(28):1305-7. Presse Med. 1995. PMID: 7501623 Review. French.

5

[Exploration of the complement system in clinical practice].

Frémeaux-Bacchi V, Blouin J, Weiss L. Frémeaux-Bacchi V, et al. Among authors: blouin j. Arch Pediatr. 1994 Jan;1(1):71-7. Arch Pediatr. 1994. PMID: 8087225 Review. French.

6

Restricted genetic defects underlie human complement C6 deficiency.

Dragon-Durey MA, Fremeaux-Bacchi V, Blouin J, Barraud D, Fridman WH, Kazatchkine MD. Dragon-Durey MA, et al. Among authors: blouin j. Clin Exp Immunol. 2003 Apr;132(1):87-91. doi: 10.1046/j.1365-2249.2003.02099.x. Clin Exp Immunol. 2003. PMID: 12653841 Free PMC article.

7

Anti-Factor H autoantibodies associated with atypical hemolytic uremic syndrome.

Dragon-Durey MA, Loirat C, Cloarec S, Macher MA, Blouin J, Nivet H, Weiss L, Fridman WH, Frémeaux-Bacchi V. Dragon-Durey MA, et al. Among authors: blouin j. J Am Soc Nephrol. 2005 Feb;16(2):555-63. doi: 10.1681/ASN.2004050380. Epub 2004 Dec 8. J Am Soc Nephrol. 2005. PMID: 15590760

8

Complete inherited deficiency of the fourth complement component in a child with systemic lupus erythematosus and his disease-free brother in a north African family.

Fremeaux-Bacchi V, Uring-Lambert B, Weiss L, Brun P, Blouin J, Hartmann D, Loirat C, Hauptmann G, Kazatchkine MD. Fremeaux-Bacchi V, et al. Among authors: blouin j. J Clin Immunol. 1994 Sep;14(5):273-9. doi: 10.1007/BF01540980. J Clin Immunol. 1994. PMID: 7814456

9

Autoantibodies to the collagen-like region of C1q are strongly associated with classical pathway-mediated hypocomplementemia in systemic lupus erythematosus.

Frémeaux-Bacchi V, Weiss L, Demouchy C, Blouin J, Kazatchkine MD. Frémeaux-Bacchi V, et al. Among authors: blouin j. Lupus. 1996 Jun;5(3):216-20. doi: 10.1177/096120339600500309. Lupus. 1996. PMID: 8803893

10

Human complement factor H deficiency associated with hemolytic uremic syndrome.

Rougier N, Kazatchkine MD, Rougier JP, Fremeaux-Bacchi V, Blouin J, Deschenes G, Soto B, Baudouin V, Pautard B, Proesmans W, Weiss E, Weiss L. Rougier N, et al. Among authors: blouin j. J Am Soc Nephrol. 1998 Dec;9(12):2318-26. doi: 10.1681/ASN.V9122318. J Am Soc Nephrol. 1998. PMID: 9848786

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